Primary Site >> Stomach Cancer
Gene >> KMT2A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118519626:118519626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11146G>A |
| AA Mutation | p.Gly3716Ser(p.G3716S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118476890:118476890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756562807 |
| CDS Mutation | c.3242G>A |
| AA Mutation | p.Arg1081Gln(p.R1081Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118501100:118501100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6263A>G |
| AA Mutation | p.Glu2088Gly(p.E2088G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118494704:118494704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5291G>A |
| AA Mutation | p.Arg1764His(p.R1764H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118472295:118472295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136C>T |
| AA Mutation | p.Ala379Val(p.A379V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118495884:118495884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5539C>T |
| AA Mutation | p.Pro1847Ser(p.P1847S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118488636:118488636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4355G>T |
| AA Mutation | p.Cys1452Phe(p.C1452F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118509143:118509143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10834G>A |
| AA Mutation | p.Ala3612Thr(p.A3612T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118493108:118493108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377724112 |
| CDS Mutation | c.5047C>T |
| AA Mutation | p.Arg1683Cys(p.R1683C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118521307:118521307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11524G>A |
| AA Mutation | p.Gly3842Ser(p.G3842S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473815:118473815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2656C>T |
| AA Mutation | p.Arg886Trp(p.R886W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118482042:118482042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3962A>C |
| AA Mutation | p.Lys1321Thr(p.K1321T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000389506 |
| Start | 118484183:118484183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4087G>A |
| AA Mutation | p.Glu1363Lys(p.E1363K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118488654:118488654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4373T>C |
| AA Mutation | p.Phe1458Ser(p.F1458S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118506121:118506121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10220C>T |
| AA Mutation | p.Pro3407Leu(p.P3407L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118472418:118472418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259G>A |
| AA Mutation | p.Arg420Gln(p.R420Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505968:118505968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149340870 |
| CDS Mutation | c.10067C>T |
| AA Mutation | p.Ala3356Val(p.A3356V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118493061:118493061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5000C>T |
| AA Mutation | p.Ala1667Val(p.A1667V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118504345:118504345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8444C>T |
| AA Mutation | p.Pro2815Leu(p.P2815L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118509180:118509180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10871C>T |
| AA Mutation | p.Ala3624Val(p.A3624V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118472913:118472913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1754T>G |
| AA Mutation | p.Leu585Arg(p.L585R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473744:118473744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2585G>A |
| AA Mutation | p.Arg862Gln(p.R862Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118506100:118506100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10199C>T |
| AA Mutation | p.Pro3400Leu(p.P3400L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118521969:118521969(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11707C>T |
| AA Mutation | p.Arg3903Cys(p.R3903C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118476832:118476832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3184T>C |
| AA Mutation | p.Ser1062Pro(p.S1062P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118501072:118501072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6235G>A |
| AA Mutation | p.Val2079Ile(p.V2079I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118504618:118504618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8717C>A |
| AA Mutation | p.Pro2906His(p.P2906H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118472667:118472667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782313746 |
| CDS Mutation | c.1508G>A |
| AA Mutation | p.Arg503Gln(p.R503Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118436528:118436528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.16C>T |
| AA Mutation | p.Arg6Trp(p.R6W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118491277:118491277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782281385 |
| CDS Mutation | c.4778G>A |
| AA Mutation | p.Arg1593His(p.R1593H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505106:118505106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9205C>T |
| AA Mutation | p.Pro3069Ser(p.P3069S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118503009:118503009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782655113 |
| CDS Mutation | c.7108C>A |
| AA Mutation | p.Leu2370Ile(p.L2370I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389506 |
| Start | 118502538:118502538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527501404 |
| CDS Mutation | c.6637A>G |
| AA Mutation | p.Met2213Val(p.M2213V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118482022:118482022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3942G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118503881:118503881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7980A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473274:118473274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2115T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505211:118505211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9310T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118503974:118503974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8073A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118481788:118481788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375849517 |
| CDS Mutation | c.3708C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118474087:118474087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2928C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118490230:118490230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4677C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473139:118473139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782676585 |
| CDS Mutation | c.1980C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473004:118473004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782608459 |
| CDS Mutation | c.1845G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505942:118505942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10041A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118511985:118511985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11097A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389506 |
| Start | 118488727:118488727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4446T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118505200:118505200(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.9304delA |
| AA Mutation | p.Ile3102SerfsTer3(p.I3102Sfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118502896:118502896(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6998delC |
| AA Mutation | p.Pro2333HisfsTer11(p.P2333Hfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118481726:118481726(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3648delA |
| AA Mutation | p.Glu1217ArgfsTer18(p.E1217Rfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473471:118473471(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2318delC |
| AA Mutation | p.Pro773ArgfsTer8(p.P773Rfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118491843:118491843(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4914delA |
| AA Mutation | p.Glu1639SerfsTer6(p.E1639Sfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118520850:118520850(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.11474delA |
| AA Mutation | p.Lys3825ArgfsTer31(p.K3825Rfs*31) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389506 |
| Start | 118473113:118473113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1954C>T |
| AA Mutation | p.Arg652Ter(p.R652*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000389506 |
| Start | 118503867:118503867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7966C>T |
| AA Mutation | p.Arg2656Ter(p.R2656*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000389506 |
| Start | 118473470:118473471(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs782297546 |
| CDS Mutation | c.2318dupC |
| AA Mutation | p.Ser774ValfsTer12(p.S774Vfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |